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FDA 510(k)

FS ACTIVATOR III

K-Number: K003185 · 2001-03-20

ApplicantActivator Methods International, Ltd.
Decision Date2001-03-20
Product CodeLXM
DecisionSubstantially Equivalent

Device Summary

FS ACTIVATOR III is the device name listed in this FDA 510(k) record. The listed applicant is Activator Methods International, Ltd.. It received FDA 510(k) clearance on 2001-03-20 under 510(k) number K003185. The device is classified under product code LXM. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FS ACTIVATOR III?

FS ACTIVATOR III is a medical device that received FDA 510(k) clearance on 2001-03-20. The listed applicant is Activator Methods International, Ltd.. The 510(k) number is K003185.

When did FS ACTIVATOR III receive FDA 510(k) clearance?

FS ACTIVATOR III received FDA 510(k) clearance on 2001-03-20, under 510(k) number K003185.

Who is the listed applicant for FS ACTIVATOR III?

The FDA 510(k) record lists Activator Methods International, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FS ACTIVATOR III?

The FDA product code for FS ACTIVATOR III is LXM.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Activator Methods International, Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K112606ACTIVATOR V-EK072519ACTIVATOR V SPINAL ADJUSTING INSTRUMENT

Related Devices (Code: LXM)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K234036SONIK MONARK 100Neuro Spinal Innovation, Inc.K192629SpinalyticsOptima Health Solutions International Corp.K172536Atlas Percussion Adjusting InstrumentSpinalight, Inc.K160278VSTAAR AdjusteRSpinal Acoustics, LLCK112606ACTIVATOR V-EActivator Methods International, Ltd.K082218MAX ADJUSTING INSTRUMENTManna Omni International, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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